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Structural role of the T94I rhodopsin mutation in congenital stationary night blindness.
Singhal, Ankita; Guo, Ying; Matkovic, Milos; Schertler, Gebhard; Deupi, Xavier; Yan, Elsa Cy; Standfuss, Joerg.
  • Singhal A; Division of Biology and Chemistry, Laboratory of Biomolecular Research, Paul Scherrer Institute, Villigen, Switzerland.
  • Guo Y; Department of Chemistry, Yale University, New Haven, CT, USA.
  • Matkovic M; Division of Biology and Chemistry, Laboratory of Biomolecular Research, Paul Scherrer Institute, Villigen, Switzerland.
  • Schertler G; Division of Biology and Chemistry, Laboratory of Biomolecular Research, Paul Scherrer Institute, Villigen, Switzerland Deparment of Biology, ETH Zurich, Zürich, Switzerland.
  • Deupi X; Division of Biology and Chemistry, Laboratory of Biomolecular Research, Paul Scherrer Institute, Villigen, Switzerland Condensed Matter Theory Group, Paul Scherrer Institute, Villigen, Switzerland.
  • Yan EC; Department of Chemistry, Yale University, New Haven, CT, USA.
  • Standfuss J; Division of Biology and Chemistry, Laboratory of Biomolecular Research, Paul Scherrer Institute, Villigen, Switzerland joerg.standfuss@psi.ch.
EMBO Rep ; 17(10): 1431-1440, 2016 10.
Article en En | MEDLINE | ID: mdl-27458239
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Rodopsina / Enfermedades Hereditarias del Ojo / Ceguera Nocturna / Enfermedades Genéticas Ligadas al Cromosoma X / Mutación / Miopía Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2016 Tipo del documento: Article
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Rodopsina / Enfermedades Hereditarias del Ojo / Ceguera Nocturna / Enfermedades Genéticas Ligadas al Cromosoma X / Mutación / Miopía Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2016 Tipo del documento: Article